Kikuko Hotta

Tondabayashicho, 5848540, Japan

Last Updated: 09/26/2026

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Found 32 publications

Ezrin works as a scaffold protein for a macrophage checkpoint molecule CD47, leading to a poor prognosis for patients with uterine cervical squamous cell carcinoma.

Ezrin works as a scaffold protein for a macrophage checkpoint molecule CD47, leading to a poor prognosis for patients with uterine cervical squamous cell carcinoma.

Journal: Taiwanese journal of obstetrics & gynecology

Published: December 03, 2024

Moesin affects the plasma membrane expression and the immune checkpoint function of CD47 in human ovarian clear cell carcinoma.

Moesin affects the plasma membrane expression and the immune checkpoint function of CD47 in human ovarian clear cell carcinoma.

Journal: Journal of reproductive immunology

Published: August 29, 2023

Identification of differentially methylated regions associated with both liver fibrosis and hepatocellular carcinoma.

Identification of differentially methylated regions associated with both liver fibrosis and hepatocellular carcinoma.

Journal: BMC gastroenterology

Published: December 02, 2022

Two differentially methylated region networks in nonalcoholic fatty liver disease, viral hepatitis, and hepatocellular carcinoma.

Two differentially methylated region networks in nonalcoholic fatty liver disease, viral hepatitis, and hepatocellular carcinoma.

Journal: BMC gastroenterology

Published: December 16, 2021

Association of protein tyrosine phosphatase 1B gene polymorphism with the effects of weight reduction therapy on bodyweight and glycolipid profiles in obese patients.

Association of protein tyrosine phosphatase 1B gene polymorphism with the effects of weight reduction therapy on bodyweight and glycolipid profiles in obese patients.

Journal: Journal of diabetes investigation

Published: May 22, 2020

Novel mutation identified in Leber congenital amaurosis - a case report.

Novel mutation identified in Leber congenital amaurosis - a case report.

Journal: BMC ophthalmology

Published: March 27, 2020

Eleven-year follow-up of a Japanese retinitis pigmentosa patient with an HK1 gene mutation.

Eleven-year follow-up of a Japanese retinitis pigmentosa patient with an HK1 gene mutation.

Journal: Ophthalmic genetics

Published: October 18, 2019

A novel compound heterozygous mutation in TTC8 identified in a Japanese patient.

A novel compound heterozygous mutation in TTC8 identified in a Japanese patient.

Journal: Human genome variation

Published: November 24, 2018

Identification of differentially methylated region (DMR) networks associated with progression of nonalcoholic fatty liver disease.

Identification of differentially methylated region (DMR) networks associated with progression of nonalcoholic fatty liver disease.

Journal: Scientific reports

Published: March 16, 2018

Identification of the genomic region under epigenetic regulation during non-alcoholic fatty liver disease progression.

Identification of the genomic region under epigenetic regulation during non-alcoholic fatty liver disease progression.

Journal: Hepatology research : the official journal of the Japan Society of Hepatology

Published: August 08, 2017

Identification of core gene networks and hub genes associated with progression of non-alcoholic fatty liver disease by RNA sequencing.

Identification of core gene networks and hub genes associated with progression of non-alcoholic fatty liver disease by RNA sequencing.

Journal: Hepatology research : the official journal of the Japan Society of Hepatology

Published: December 16, 2016

Characteristics of non-obese non-alcoholic fatty liver disease: Effect of genetic and environmental factors.

Characteristics of non-obese non-alcoholic fatty liver disease: Effect of genetic and environmental factors.

Journal: Hepatology research : the official journal of the Japan Society of Hepatology

Published: November 04, 2015

Showing 1-12 of 32

Last Updated: 09/26/2026